QC Analyst

TN United Kingdom; Liverpool; On-site; GBP 25,000 - 35,000; Full time

Job summary

A well-established pharmaceutical manufacturer in Liverpool is seeking a QC Analyst to ensure the safety and compliance of products through rigorous analytical testing. The ideal candidate will have a BSc in Chemistry or related fields and experience in a GMP-regulated environment. Join a supportive team with opportunities for professional development.

Benefits

Professional Development

Ongoing Training

Career Progression

Qualifications

• 1-3 years of experience in a GMP-regulated pharmaceutical laboratory.
• Proficient in HPLC; experience with other analytical chemistry techniques is advantageous.

Responsibilities

• Conduct routine and non-routine testing of raw materials and finished products.
• Operate and maintain analytical instruments including HPLC, GC, ICP.
• Ensure strict adherence to cGMP and internal quality standards.

Skills

Attention to Detail

Analytical Skills

Education

BSc in Chemistry

BSc in Pharmaceutical Sciences

Tools

HPLC

GC

ICP

Wet Chemistry

Titrations

Job description

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Our client is a well-established, sterile GMP-accredited pharmaceutical manufacturer based in Liverpool, known for producing high-quality pharmaceutical products for both UK and international markets, exporting products to over 20 countries worldwide.
Are you a skilled QC Analyst with a passion for pharmaceutical quality and compliance? Do you thrive in a GMP-regulated environment and enjoy working with advanced analytical techniques? If so, we want to hear from you!

QC Analyst
Liverpool

As a QC Analyst, you will play a key role in ensuring the safety, efficacy, and compliance of pharmaceutical products through rigorous analytical testing.

The responsibilities of the QC Analyst include:

•Conduct routine and non-routine testing of raw materials and finished pharmaceutical products.
•Operate and maintain analytical instruments including HPLC, GC, ICP, wet chemistry and titrations.
•Assist in the introduction and validation of new methods and equipment
•Assist laboratory manager and technical managers in the capacity as a technical specialist providing advice and technical detail for routine analysis
•Perform equipment calibration and ensure accurate documentation.
•Assist in the investigation and documention of Out of Specification (OOS) and Out of Trend (OOT) results.
•Ensure strict adherence to cGMP and internal quality standards.
•Compile, interpret, and report analytical data for R&D and regulatory purposes.

The ideal candidate for the QC Analyst post will have:

•BSc (or higher) in Chemistry, Pharmaceutical Sciences, or a related discipline.
•1–3 years of experience in a GMP-regulated pharmaceutical laboratory.
•Proficient in HPLC; experience with other analytical chemistry techniques is advantageous.
•Strong attention to detail and ability to work independently.
•Familiarity with regulatory guidelines (MHRA, FDA, ICH) is a plus.

In return, you’ll join a supportive team with opportunities for professional development, ongoing training, and career progression within a growing pharmaceutical business.